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日期:2024-08-04
Fabry disease (/ˈfɑːbri/) (also known as Fabry's disease, Anderson- Fabry disease, angiokeratoma corpori ......
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日期:2024-08-07
Anderson-Fabry Disease is also known as Fabry's disease; alpha-galactosidase.
Anderson-Fabry Disease is a ......
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日期:2024-08-05
Fabry disease is an X-linked lysosomal disorder that leads to excessive deposition of neutral glycosphingolipids in the vascular endothelium of several organs and in epithelial and smooth muscle cells. Progressive endothelial accumulation of glycosphingol...
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日期:2024-08-11
301500 - FABRY DISEASE - ANGIOKERATOMA CORPORIS DIFFUSUM;; ANDERSON-FABRY DISEASE;; HEREDITARY DYSTOPIC LIPIDOSIS;; ALPHA-GALACTOSIDASE A DEFICIENCY;; GLA DEFICIENCY;; CERAMIDE TRIHEXOSIDASE ... ......
Orphanet Journal of Rare Diseases | Full text | Long term enzyme replacement therapy for Fabry disea
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日期:2024-08-08
Fabry disease is an X-linked lysosomal storage disorder caused by α-galactosidase A deficiency leading to renal, cardiac, cerebrovascular disease and premature death. Treatment with α-galactosidase A (enzyme replacement therapy, ERT) stabilises disease in...
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日期:2024-08-04
2014年9月29日 - Treatment & Management: Genetics of Fabry Disease. Fabry disease is an X- linked lysosomal storage disease that is caused by deficient ......
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日期:2024-08-05
Fabry disease (also known as Fabry's disease, Anderson-Fabry disease, angiokeratoma corporis diffusum, and alpha-galactosidase A deficiency) is a rare ......
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日期:2024-08-09
Learn about Fabry disease, an inherited disorder caused by deficiency of the alpha-galactosidase A enzyme, and Fabrazyme enzyme replacement therapy. ... Welcome to Fabrazyme.com Fabry disease is an inherited disorder caused by the deficiency of an ......